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Adinizer

FDA UDI

Class II (US FDA UDI)

by Bsl Co.

Identity

Trade Name
Adinizer FDA UDI
Generic Name
Autologous adipose tissue reinjection set FDA UDI
Model / Reference
SKT-AN-24201 FDA UDI

Identifiers

Primary DI / UDI-DI
08800080202217 FDA UDI
FDA Product Code
QKL FDA UDI
GMDN Term
Autologous adipose tissue reinjection set FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Autologous adipose tissue reinjection set

Adinizer by Bsl Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Autologous adipose tissue reinjection set.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bsl Co.

Sources (1)

  • FDA UDI 6e3b9f8a-55d3-42ae-a8ea-17355302aa17 34 fields · synced Jun 8, 2026